• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

增强 TRAIL 诱导剂 ONC201 的剂量可抑制转移并促进肿瘤内 NK 细胞募集。

Dose intensification of TRAIL-inducing ONC201 inhibits metastasis and promotes intratumoral NK cell recruitment.

机构信息

Laboratory of Translational Oncology and Experimental Cancer Therapeutics, Molecular Therapeutics Program and Department of Hematology/Oncology.

Blood Cell Development and Function Program, Institute for Cancer Research.

出版信息

J Clin Invest. 2018 Jun 1;128(6):2325-2338. doi: 10.1172/JCI96711. Epub 2018 Apr 30.

DOI:10.1172/JCI96711
PMID:29533922
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5983321/
Abstract

ONC201 is a first-in-class, orally active antitumor agent that upregulates cytotoxic TRAIL pathway signaling in cancer cells. ONC201 has demonstrated safety and preliminary efficacy in a first-in-human trial in which patients were dosed every 3 weeks. We hypothesized that dose intensification of ONC201 may impact antitumor efficacy. We discovered that ONC201 exerts dose- and schedule-dependent effects on tumor progression and cell death signaling in vivo. With dose intensification, we note a potent anti-metastasis effect and inhibition of cancer cell migration and invasion. Our preclinical results prompted a change in ONC201 dosing in all open clinical trials. We observed accumulation of activated NK+ and CD3+ cells within ONC201-treated tumors and that NK cell depletion inhibits ONC201 efficacy in vivo, including against TRAIL/ONC201-resistant Bax-/- tumors. Immunocompetent NCR1-GFP mice, in which NK cells express GFP, demonstrated GFP+ NK cell infiltration of syngeneic MC38 colorectal tumors. Activation of primary human NK cells and increased degranulation occurred in response to ONC201. Coculture experiments identified a role for TRAIL in human NK-mediated antitumor cytotoxicity. Preclinical results indicate the potential utility for ONC201 plus anti-PD-1 therapy. We observed an increase in activated TRAIL-secreting NK cells in the peripheral blood of patients after ONC201 treatment. The results offer what we believe to be a unique pathway of immune stimulation for cancer therapy.

摘要

ONC201 是一种首创的、口服活性抗肿瘤药物,可上调癌细胞中细胞毒性 TRAIL 通路信号。ONC201 在首次人体试验中表现出安全性和初步疗效,患者每 3 周给药一次。我们假设 ONC201 的剂量强化可能会影响抗肿瘤疗效。我们发现,ONC201 对体内肿瘤进展和细胞死亡信号具有剂量和方案依赖性的影响。随着剂量强化,我们注意到一种强大的抗转移作用以及对癌细胞迁移和侵袭的抑制作用。我们的临床前结果促使所有开放临床试验改变 ONC201 的剂量。我们观察到在 ONC201 治疗的肿瘤内积累了活化的 NK+和 CD3+细胞,并且 NK 细胞耗竭抑制了 ONC201 在体内的疗效,包括对 TRAIL/ONC201 耐药 Bax-/-肿瘤的疗效。在 NK 细胞表达 GFP 的免疫功能正常的 NCR1-GFP 小鼠中,观察到 GFP+NK 细胞浸润同种异体 MC38 结直肠肿瘤。ONC201 引起原代人 NK 细胞的活化和脱颗粒增加。共培养实验确定了 TRAIL 在人 NK 介导的抗肿瘤细胞毒性中的作用。临床前结果表明 ONC201 加抗 PD-1 治疗具有潜在的应用价值。我们观察到 ONC201 治疗后患者外周血中活化的分泌 TRAIL 的 NK 细胞增加。这些结果提供了我们认为是癌症治疗中一种独特的免疫刺激途径。

相似文献

1
Dose intensification of TRAIL-inducing ONC201 inhibits metastasis and promotes intratumoral NK cell recruitment.增强 TRAIL 诱导剂 ONC201 的剂量可抑制转移并促进肿瘤内 NK 细胞募集。
J Clin Invest. 2018 Jun 1;128(6):2325-2338. doi: 10.1172/JCI96711. Epub 2018 Apr 30.
2
Small-Molecule ONC201/TIC10 Targets Chemotherapy-Resistant Colorectal Cancer Stem-like Cells in an Akt/Foxo3a/TRAIL-Dependent Manner.小分子 ONC201/TIC10 通过 Akt/Foxo3a/TRAIL 依赖的方式靶向化疗耐药结直肠肿瘤干细胞。
Cancer Res. 2015 Apr 1;75(7):1423-32. doi: 10.1158/0008-5472.CAN-13-3451. Epub 2015 Feb 20.
3
Anti-tumor effects of ONC201 in combination with VEGF-inhibitors significantly impacts colorectal cancer growth and survival in vivo through complementary non-overlapping mechanisms.ONC201 联合 VEGF 抑制剂的抗肿瘤作用通过互补且非重叠的机制显著影响结直肠癌的体内生长和存活。
J Exp Clin Cancer Res. 2018 Jan 22;37(1):11. doi: 10.1186/s13046-018-0671-0.
4
ONC201 Demonstrates Antitumor Effects in Both Triple-Negative and Non-Triple-Negative Breast Cancers through TRAIL-Dependent and TRAIL-Independent Mechanisms.ONC201通过依赖TRAIL和不依赖TRAIL的机制在三阴性和非三阴性乳腺癌中均表现出抗肿瘤作用。
Mol Cancer Ther. 2017 Jul;16(7):1290-1298. doi: 10.1158/1535-7163.MCT-17-0121. Epub 2017 Apr 19.
5
Preclinical evaluation of the imipridone family, analogs of clinical stage anti-cancer small molecule ONC201, reveals potent anti-cancer effects of ONC212.临床阶段抗癌小分子 ONC201 的类似物 imipridone 家族的临床前评估显示 ONC212 具有强大的抗癌作用。
Cell Cycle. 2017 Oct 2;16(19):1790-1799. doi: 10.1080/15384101.2017.1325046. Epub 2017 May 10.
6
Identification of TRAIL-inducing compounds highlights small molecule ONC201/TIC10 as a unique anti-cancer agent that activates the TRAIL pathway.可诱导TRAIL的化合物的鉴定突出了小分子ONC201/TIC10作为一种激活TRAIL途径的独特抗癌剂。
Mol Cancer. 2015 May 1;14:99. doi: 10.1186/s12943-015-0346-9.
7
ONC201 induces cell death in pediatric non-Hodgkin's lymphoma cells.ONC201可诱导小儿非霍奇金淋巴瘤细胞死亡。
Cell Cycle. 2015 Aug 3;14(15):2422-8. doi: 10.1080/15384101.2015.1054086. Epub 2015 Jun 1.
8
Small Molecular TRAIL Inducer ONC201 Induces Death in Lung Cancer Cells: A Preclinical Study.小分子 TRAIL 诱导剂 ONC201 诱导肺癌细胞死亡:一项临床前研究。
PLoS One. 2016 Sep 14;11(9):e0162133. doi: 10.1371/journal.pone.0162133. eCollection 2016.
9
Combination of ONC201 and TLY012 induces selective, synergistic apoptosis in vitro and significantly delays PDAC xenograft growth in vivo.ONC201 与 TLY012 的联合使用在体外诱导选择性协同凋亡,并显著延缓体内 PDAC 异种移植物的生长。
Cancer Biol Ther. 2021 Dec 2;22(10-12):607-618. doi: 10.1080/15384047.2021.1976567.
10
ONC201 kills solid tumor cells by triggering an integrated stress response dependent on ATF4 activation by specific eIF2α kinases.ONC201通过触发一种依赖于特定eIF2α激酶激活ATF4的综合应激反应来杀死实体瘤细胞。
Sci Signal. 2016 Feb 16;9(415):ra18. doi: 10.1126/scisignal.aac4374.

引用本文的文献

1
Combination of LowDose Epigenetic Modifiers and TIC10 for the Activation of Antitumor Immunity and Inhibition of Tumor Growth in Gastrointestinal Cancer.低剂量表观遗传修饰剂与TIC10联合用于激活抗肿瘤免疫及抑制胃肠道肿瘤生长
Cancer Med. 2025 Jul;14(14):e71061. doi: 10.1002/cam4.71061.
2
Dose Optimization of ClpP Agonists Using an In Vitro Microfluidic Perfusion Platform and In Silico Pharmacokinetic-Pharmacodynamic Modeling.使用体外微流控灌注平台和计算机模拟药代动力学-药效学模型对ClpP激动剂进行剂量优化
AAPS J. 2025 Jun 13;27(4):109. doi: 10.1208/s12248-025-01088-9.
3
Imipridones ONC201/ONC206 + RT/TMZ triple (IRT) therapy reduces intracranial tumor burden, prolongs survival in orthotopic IDH-WT GBM mouse model, and suppresses MGMT.咪吡酮类药物ONC201/ONC206联合放疗/替莫唑胺三联(IRT)疗法可减轻颅内肿瘤负担,延长原位异柠檬酸脱氢酶野生型胶质母细胞瘤小鼠模型的生存期,并抑制O6-甲基鸟嘌呤-DNA甲基转移酶(MGMT)。
Oncotarget. 2025 Mar 27;16:230-248. doi: 10.18632/oncotarget.28707.
4
TRAIL agonists rescue mice from radiation-induced lung, skin, or esophageal injury.肿瘤坏死因子相关凋亡诱导配体(TRAIL)激动剂可使小鼠免受辐射引起的肺部、皮肤或食管损伤。
J Clin Invest. 2025 Jan 14;135(5):e173649. doi: 10.1172/JCI173649.
5
Synergistic combination therapy with ONC201 or ONC206, and enzalutamide or darolutamide in preclinical studies of castration-resistant prostate cancer.在去势抵抗性前列腺癌的临床前研究中,ONC201或ONC206与恩杂鲁胺或达罗他胺的协同联合治疗。
Am J Cancer Res. 2024 Dec 25;14(12):6012-6036. doi: 10.62347/VJMW4904. eCollection 2024.
6
The mitochondrial protease ClpP is a druggable target that controls VSMC phenotype by a SIRT1-dependent mechanism.线粒体蛋白酶 ClpP 是一个可药物治疗的靶点,它通过 SIRT1 依赖的机制控制 VSMC 表型。
Redox Biol. 2024 Jul;73:103203. doi: 10.1016/j.redox.2024.103203. Epub 2024 May 21.
7
Death receptors 4/5 mediate tumour sensitivity to natural killer cell-mediated cytotoxicity in mismatch repair deficient colorectal cancer.死亡受体 4/5 介导错配修复缺陷的结直肠癌细胞对自然杀伤细胞介导的细胞毒性的敏感性。
Br J Cancer. 2024 Jul;131(2):334-346. doi: 10.1038/s41416-024-02673-z. Epub 2024 May 25.
8
Nivolumab plus ONC201 plus in microsatellite stable (MSS) metastatic colorectal cancer (mCRC) patients: a Brown University Oncology Research Group phase Ib/II study (BrUOG379).纳武利尤单抗联合ONC201治疗微卫星稳定(MSS)转移性结直肠癌(mCRC)患者:布朗大学肿瘤研究小组Ib/II期研究(BrUOG379)
Transl Gastroenterol Hepatol. 2024 Mar 15;9:15. doi: 10.21037/tgh-23-69. eCollection 2024.
9
The oncolytic adenovirus Delta-24-RGD in combination with ONC201 induces a potent antitumor response in pediatric high-grade and diffuse midline glioma models.溶瘤腺病毒 Delta-24-RGD 联合 ONC201 在小儿高级别和弥漫中线脑胶质瘤模型中诱导强烈的抗肿瘤反应。
Neuro Oncol. 2024 Aug 5;26(8):1509-1525. doi: 10.1093/neuonc/noae066.
10
Gemcitabine elaidate and ONC201 combination therapy for inhibiting pancreatic cancer in a KRAS mutated syngeneic mouse model.反油酸吉西他滨与ONC201联合疗法在KRAS突变同基因小鼠模型中对胰腺癌的抑制作用
Cell Death Discov. 2024 Mar 29;10(1):158. doi: 10.1038/s41420-024-01920-9.

本文引用的文献

1
First-in-Human Clinical Trial of Oral ONC201 in Patients with Refractory Solid Tumors.口服ONC201用于难治性实体瘤患者的首次人体临床试验。
Clin Cancer Res. 2017 Aug 1;23(15):4163-4169. doi: 10.1158/1078-0432.CCR-16-2658. Epub 2017 Mar 22.
2
Discovery and clinical introduction of first-in-class imipridone ONC201.一流的咪吡二酮ONC201的发现与临床应用
Oncotarget. 2016 Nov 8;7(45):74380-74392. doi: 10.18632/oncotarget.11814.
3
mTOR inhibition sensitizes ONC201-induced anti-colorectal cancer cell activity.mTOR抑制增强了ONC201诱导的抗结肠癌细胞活性。
Biochem Biophys Res Commun. 2016 Sep 30;478(4):1515-20. doi: 10.1016/j.bbrc.2016.08.126. Epub 2016 Aug 24.
4
The preclinical evaluation of TIC10/ONC201 as an anti-pancreatic cancer agent.TIC10/ONC201作为一种抗胰腺癌药物的临床前评估。
Biochem Biophys Res Commun. 2016 Aug 5;476(4):260-266. doi: 10.1016/j.bbrc.2016.05.106. Epub 2016 May 24.
5
ONC201 kills solid tumor cells by triggering an integrated stress response dependent on ATF4 activation by specific eIF2α kinases.ONC201通过触发一种依赖于特定eIF2α激酶激活ATF4的综合应激反应来杀死实体瘤细胞。
Sci Signal. 2016 Feb 16;9(415):ra18. doi: 10.1126/scisignal.aac4374.
6
ATF4 induction through an atypical integrated stress response to ONC201 triggers p53-independent apoptosis in hematological malignancies.通过对ONC201的非典型综合应激反应诱导ATF4可引发血液系统恶性肿瘤中不依赖p53的凋亡。
Sci Signal. 2016 Feb 16;9(415):ra17. doi: 10.1126/scisignal.aac4380.
7
First-In-Class Small Molecule ONC201 Induces DR5 and Cell Death in Tumor but Not Normal Cells to Provide a Wide Therapeutic Index as an Anti-Cancer Agent.首创小分子ONC201在肿瘤细胞而非正常细胞中诱导DR5表达和细胞死亡,作为一种抗癌药物具有广泛的治疗指数。
PLoS One. 2015 Nov 18;10(11):e0143082. doi: 10.1371/journal.pone.0143082. eCollection 2015.
8
Identification of TRAIL-inducing compounds highlights small molecule ONC201/TIC10 as a unique anti-cancer agent that activates the TRAIL pathway.可诱导TRAIL的化合物的鉴定突出了小分子ONC201/TIC10作为一种激活TRAIL途径的独特抗癌剂。
Mol Cancer. 2015 May 1;14:99. doi: 10.1186/s12943-015-0346-9.
9
Small-Molecule ONC201/TIC10 Targets Chemotherapy-Resistant Colorectal Cancer Stem-like Cells in an Akt/Foxo3a/TRAIL-Dependent Manner.小分子 ONC201/TIC10 通过 Akt/Foxo3a/TRAIL 依赖的方式靶向化疗耐药结直肠肿瘤干细胞。
Cancer Res. 2015 Apr 1;75(7):1423-32. doi: 10.1158/0008-5472.CAN-13-3451. Epub 2015 Feb 20.
10
Genetic and Pharmacological Screens Converge in Identifying FLIP, BCL2, and IAP Proteins as Key Regulators of Sensitivity to the TRAIL-Inducing Anticancer Agent ONC201/TIC10.遗传和药理学筛选共同确定FLIP、BCL2和IAP蛋白是对TRAIL诱导的抗癌药物ONC201/TIC10敏感性的关键调节因子。
Cancer Res. 2015 Apr 15;75(8):1668-74. doi: 10.1158/0008-5472.CAN-14-2356. Epub 2015 Feb 13.